[mira_talk] Re: FW: 454 assembly

  • From: Thomas Müller <thomas.mueller@xxxxxxxxxxxxxxxx>
  • To: mira_talk@xxxxxxxxxxxxx
  • Date: Thu, 22 Jul 2010 11:48:52 +0200

Sorry my bad!!!
I meant:

--job=denovo,genome,draft,454

cheers
Thomas


On Jul 22, 2010, at 11:36 AM, Shabhonam Caim (TGAC) wrote:

> Thanks thomas for your reply but still I am getting error:
> I have used the following command and provided the qual file as well :
>  
> mira --project=test --job=denovo,genome,draft 454_SETTINGS 
> -FN:fai=2.GAC.454Reads.fna -FN:fqui=2.GAC.454Reads.qual
>  
>             Minimum reads per group needed for tagging (mrpg)    :  [san]  2
>                                                                     [454]  4
>             Minimum neighbour quality needed for tagging (mnq)   :  [san]  20
>                                                                     [454]  20
>             Minimum Group Quality needed for RMB Tagging (mgqrt) :  [san]  30
>                                                                     [454]  25
>             End-read Marking Exclusion Area in bases (emea)      :  [san]  25
>                                                                     [454]  10
>             Also mark gap bases (amgb)                           :  [san]  yes
>                                                                     [454]  no
>                 Also mark gap bases - even multicolumn (amgbemc) :  [san]  yes
>                                                                     [454]  yes
>                 Also mark gap bases - need both strands (amgbnbs):  [san]  yes
>                                                                     [454]  yes
>         Force non-IUPAC consensus per sequencing type (fnicpst)  :  [san]  no
>                                                                     [454]  no
>         Merge short reads (msr)                                  :  [san]  no
>                                                                     [454]  no
>         Gap override ratio (gor)                                 :  [san]  66
>                                                                     [454]  66
>  
>   Edit options (-ED):
>         Automatic contig editing (ace)              :  [san]  no
>                                                        [454]  yes
>      Sanger only:
>         Strict editing mode (sem)                   : no
>         Confirmation threshold in percent (ct)      : 50
>  
>   Directories (-DI):
>         When loading EXP files            :
>         When loading SCF files            :
>         Top directory for writing files   : test_assembly
>         For writing result files          : test_assembly/test_d_results
>         For writing result info files     : test_assembly/test_d_info
>         For writing log files             : test_assembly/test_d_log
>         For writing checkpoint files      : test_assembly/test_d_chkpt
>  
>   File names (-FN):
>         When loading sequences from FASTA            :  [san]  
> test_in.sanger.fasta
>                                                         [454]  
> 2.GAC.454Reads.fna
>         When loading qualities from FASTA quality    :  [san]  
> test_in.sanger.fasta.qual
>                                                         [454]  
> 2.GAC.454Reads.qual
>         When loading sequences from FASTQ            :  [san]  
> test_in.sanger.fastq
>                                                         [454]  
> test_in.454.fastq
>         When loading project from CAF                : test_in.sanger.caf
>         When loading project from MAF (disabled)     : test_in.sanger.maf
>         When loading EXP fofn                        : test_in.fofn
>         When loading project from PHD                : test_in.phd.1
>         When loading strain data                     : test_straindata_in.txt
>         When loading XML trace info files            :  [san]  
> test_traceinfo_in.sanger.xml
>                                                         [454]  
> test_traceinfo_in.454.xml
>         When loading SSAHA vector screen results     : 
> test_ssaha2vectorscreen_in.txt
>  
>         When loading backbone from MAF               : test_backbone_in.maf
>         When loading backbone from CAF               : test_backbone_in.caf
>         When loading backbone from GenBank           : test_backbone_in.gbf
>         When loading backbone from FASTA             : test_backbone_in.fasta
>  
>  
>   Output files (-OUTPUT/-OUT):
>         Save simple singlets in project (sssip)      :  [san]  no
>                                                         [454]  no
>         Save tagged singlets in project (stsip)      :  [san]  yes
>                                                         [454]  yes
>  
>         Remove rollover logs (rrol)                  : yes
>         Remove log directory (rld)                   : no
>  
>     Result files:
>         Saved as CAF                       (orc)     : yes
>         Saved as FASTA                     (orf)     : yes
>         Saved as GAP4 (directed assembly)  (org)     : no
>         Saved as phrap ACE                 (ora)     : yes
>         Saved as HTML                      (orh)     : no
>         Saved as Transposed Contig Summary (ors)     : yes
>         Saved as simple text format        (ort)     : no
>         Saved as wiggle                    (orw)     : yes
>  
>     Temporary result files:
>         Saved as CAF                       (otc)     : yes
>         Saved as CAF                       (otm)     : no
>         Saved as FASTA                     (otf)     : no
>         Saved as GAP4 (directed assembly)  (otg)     : no
>         Saved as phrap ACE                 (ota)     : no
>         Saved as HTML                      (oth)     : no
>         Saved as Transposed Contig Summary (ots)     : no
>         Saved as simple text format        (ott)     : no
>  
>     Extended temporary result files:
>         Saved as CAF                      (oetc)     : no
>         Saved as FASTA                    (oetf)     : no
>         Saved as GAP4 (directed assembly) (oetg)     : no
>         Saved as phrap ACE                (oeta)     : no
>         Saved as HTML                     (oeth)     : no
>         Save also singlets               (oetas)     : no
>  
>     Alignment output customisation:
>         TEXT characters per line (tcpl)              : 60
>         HTML characters per line (hcpl)              : 60
>         TEXT end gap fill character (tegfc)          :
>         HTML end gap fill character (hegfc)          :
>  
>     File / directory output names:
>         CAF             : test_out.caf
>         MAF             : test_out.maf
>         FASTA           : test_out.unpadded.fasta
>         FASTA quality   : test_out.unpadded.fasta.qual
>         FASTA (padded)  : test_out.padded.fasta
>         FASTA qual.(pad): test_out.padded.fasta.qual
>         GAP4 (directory): test_out.gap4da
>         ACE             : test_out.ace
>         HTML            : test_out.html
>         Simple text     : test_out.txt
>         TCS overview    : test_out.tcs
>         Wiggle          : test_out.wig
> ------------------------------------------------------------------------------
> Deleting old directory test_assembly ... done.
> Creating directory test_assembly ... done.
> Creating directory test_assembly/test_d_log ... done.
> Creating directory test_assembly/test_d_results ... done.
> Creating directory test_assembly/test_d_info ... done.
> Creating directory test_assembly/test_d_chkpt ... done.
> Localtime: Thu Jul 22 10:31:49 2010
>  
>  
>  
> ========================== Memory self assessment 
> ==============================
> Running in 64 bit mode.
>  
> Dump from /proc/meminfo
> --------------------------------------------------------------------------------
> MemTotal:      8174224 kB
> MemFree:         94968 kB
> Buffers:          4644 kB
> Cached:        4976444 kB
> SwapCached:     287504 kB
> Active:        6618732 kB
> Inactive:      1307228 kB
> HighTotal:           0 kB
> HighFree:            0 kB
> LowTotal:      8174224 kB
> LowFree:         94968 kB
> SwapTotal:     2031608 kB
> SwapFree:      1476740 kB
> Dirty:            1984 kB
> Writeback:           0 kB
> AnonPages:     2936468 kB
> Mapped:          32408 kB
> Slab:            81840 kB
> PageTables:      37252 kB
> NFS_Unstable:        0 kB
> Bounce:              0 kB
> CommitLimit:   6118720 kB
> Committed_AS:  5290616 kB
> VmallocTotal: 34359738367 kB
> VmallocUsed:    263728 kB
> VmallocChunk: 34359474579 kB
> HugePages_Total:     0
> HugePages_Free:      0
> HugePages_Rsvd:      0
> Hugepagesize:     2048 kB
> --------------------------------------------------------------------------------
>  
> Dump from /proc/self/status
> --------------------------------------------------------------------------------
> Name:   mira
> State:  R (running)
> SleepAVG:       0%
> Tgid:   6158
> Pid:    6158
> PPid:   17617
> TracerPid:      0
> Uid:    8395    8395    8395    8395
> Gid:    3658    3658    3658    3658
> FDSize: 256
> Groups: 3658
> VmPeak:     4972 kB
> VmSize:     4920 kB
> VmLck:         0 kB
> VmHWM:      1744 kB
> VmRSS:      1744 kB
> VmData:      464 kB
> VmStk:        84 kB
> VmExe:      4336 kB
> VmLib:         0 kB
> VmPTE:        28 kB
> StaBrk: 00a7e000 kB
> Brk:    017f0000 kB
> StaStk: 7fffc798fa70 kB
> Threads:        1
> SigQ:   0/71680
> SigPnd: 0000000000000000
> ShdPnd: 0000000000000000
> SigBlk: 0000000000000000
> SigIgn: 0000000000000000
> SigCgt: 0000000180000000
> CapInh: 0000000000000000
> CapPrm: 0000000000000000
> CapEff: 0000000000000000
> Cpus_allowed:   
> 00000000,00000000,00000000,00000000,00000000,00000000,00000000,000000ff
> Mems_allowed:   00000000,00000001
> --------------------------------------------------------------------------------
>  
> Information on current assembly object:
>  
> AS_readpool: 0 reads.
> AS_contigs: 0 contigs.
> AS_bbcontigs: 0 contigs.
> Mem used for reads: 112 (112 B)
>  
> Memory used in assembly structures:
>                                            Eff. Size   Free cap. LostByAlign
>      AS_writtenskimhitsperid:          0        24 B         0 B         0 B
>                AS_skim_edges:          0        24 B         0 B         0 B
>                  AS_adsfacts:          0        24 B         0 B         0 B
>           AS_confirmed_edges:          0        24 B         0 B         0 B
>    AS_permanent_overlap_bans:          0        24 B         0 B         0 B
>               AS_readhitmiss:          0        24 B         0 B         0 B
>             AS_readhmcovered:          0        24 B         0 B         0 B
>                 AS_count_rhm:          0        24 B         0 B         0 B
>                  AS_clipleft:          0        24 B         0 B         0 B
>                 AS_clipright:          0        24 B         0 B         0 B
>                  AS_used_ids:          0        24 B         0 B         0 B
>               AS_multicopies:          0        24 B         0 B         0 B
>             AS_hasmcoverlaps:          0        24 B         0 B         0 B
>        AS_maxcoveragereached:          0        24 B         0 B         0 B
>        AS_coverageperseqtype:          0        24 B         0 B         0 B
>            AS_istroublemaker:          0        24 B         0 B         0 B
>                  AS_isdebris:          0        24 B         0 B         0 B
>           AS_needalloverlaps:          0        40 B         0 B         0 B
>     AS_readsforrepeatresolve:          0        40 B         0 B         0 B
>                 AS_allrmbsok:          0        24 B         0 B         0 B
>         AS_probablermbsnotok:          0        24 B         0 B         0 B
>             AS_weakrmbsnotok:          0        24 B         0 B         0 B
>           AS_readmaytakeskim:          0        40 B         0 B         0 B
>                AS_skimstaken:          0        40 B         0 B         0 B
>           AS_numskimoverlaps:          0        24 B         0 B         0 B
>        AS_numleftextendskims:          0        24 B         0 B         0 B
>          AS_rightextendskims:          0        24 B         0 B         0 B
>       AS_skimleftextendratio:          0        24 B         0 B         0 B
>      AS_skimrightextendratio:          0        24 B         0 B         0 B
>              AS_usedlogfiles:          1        48 B         0 B         0 B
> Total: 920 (920 B)
>  
> ================================================================================
> Dynamic allocs: 0
> Align allocs: 0
>  
> Fatal Error (may be due to problems of the input data):
> "You did not specify any input sequences to be loaded."
>  
> ->Thrown: void Assembly::loadSequenceData_new()
>  
> ->Caught: main
>  
> Cheers
> Shab
>  
>  
> From: mira_talk-bounce@xxxxxxxxxxxxx [mailto:mira_talk-bounce@xxxxxxxxxxxxx] 
> On Behalf Of Thomas Müller
> Sent: 22 July 2010 10:12
> To: mira_talk@xxxxxxxxxxxxx
> Subject: [mira_talk] Re: FW: 454 assembly
>  
> try:
> mira --project=test --job=denovo,genome,draft,est 454_SETTINGS 
> -FN:fai=2.GAC.454Reads.fna
>  
> But you should really also add the .qual file with FN:fqui=2.GAC.454Reads.qual
>  
> cheers
> Thomas
>  
> On Jul 22, 2010, at 10:53 AM, Shabhonam Caim (TGAC) wrote:
> 
> 
>  
> Hello Mira Users
>  
> I am trying to assemble the 454 reads using Mira by using following command:
> mira-3.0.0 mira --project=test --job=denovo,genome,draft,2.GAC.454Reads.fna
>  
> and I am getting the following error:
>  
> This is MIRA V3.0.0 (production version).
>  
> Please cite: Chevreux, B., Wetter, T. and Suhai, S. (1999), Genome Sequence
> Assembly Using Trace Signals and Additional Sequence Information.
> Computer Science and Biology: Proceedings of the German Conference on
> Bioinformatics (GCB) 99, pp. 45-56.
>  
> Mail general questions to the MIRA talk mailing list:
>         mira_talk@xxxxxxxxxxxxx
>  
> To (un-)subsubcribe the MIRA mailing lists, see:
>         http://www.chevreux.org/mira_mailinglists.html
>  
> To report bugs or ask for features, please use the new ticketing system at:
>         http://sourceforge.net/apps/trac/mira-assembler/
> This ensures that requests don't get lost.
>  
>  
> Compiled by: bach
> Sun Jan 31 20:23:36 CET 2010
> On: Linux arcadia64 2.6.27-11-generic #1 SMP Wed Apr 1 20:53:41 UTC 2009 
> x86_64 GNU/Linux
> Compiled in boundtracking mode.
> Compiled in bugtracking mode.
> Compilation settings (sorry, for debug):
>         Size of size_t  : 8
>         Size of uint32  : 4
>         Size of uint32_t: 4
>         Size of uint64  : 8
>         Size of uint64_t: 8
> Current system: Linux n57140 2.6.18-92.el5 #1 SMP Tue Apr 29 13:16:15 EDT 
> 2008 x86_64 x86_64 x86_64 GNU/Linux
>  
>  
>  
> Parsing parameters: --project=454asembly --job=denovo, genome, draft 
> pk.454.fasta
>  
> Seen no assembly quality in job definition, assuming 'normal'.
> Seen no assembly type in job definition, assuming 'genome'.
>  
> ,..
>  
> ========================= Parameter parsing error(s) 
> ==========================
>  
> * Parameter section: '(none)'
> *       unrecognised string or unexpected character: genome
>  
> * Parameter section: '(none)'
> *       unrecognised string or unexpected character: draft
>  
> * Parameter section: '(none)'
> *       unrecognised string or unexpected character: pk
>  
> * Parameter section: '(none)'
> *       unrecognised string or unexpected character: 454
>  
> * Parameter section: '(none)'
> *       unrecognised string or unexpected character: fasta
>  
> ===============================================================================
>  
> Fatal Error (may be due to problems of the input data):
> "Error while parsing parameters, sorry."
>  
> ->Thrown: void MIRAParameters::parse(istream & is, vector<MIRAParameters> & 
> Pv, MIRAParameters * singlemp)
>  
> ->Caught: main
>  
> Or can I please get the commands to run the 454 assembly (basic denovo 
> assembly with default parameters)
>  
> cheers
>  
> Shab
>  
>  
> --
> Crop Plant Biodiversity and Breeding Informatics Group (350b)
> Institute of Plant Breeding, Seed Science and Population Genetics
> University of Hohenheim
> Fruwirthstrasse 21
> D-70599 Stuttgart
> Phone: +49-711-459 24293
>  

--
Crop Plant Biodiversity and Breeding Informatics Group (350b)
Institute of Plant Breeding, Seed Science and Population Genetics
University of Hohenheim
Fruwirthstrasse 21
D-70599 Stuttgart
Phone: +49-711-459 24293

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